CA1283901C - Lubricating composition and method - Google Patents
Lubricating composition and methodInfo
- Publication number
- CA1283901C CA1283901C CA000524630A CA524630A CA1283901C CA 1283901 C CA1283901 C CA 1283901C CA 000524630 A CA000524630 A CA 000524630A CA 524630 A CA524630 A CA 524630A CA 1283901 C CA1283901 C CA 1283901C
- Authority
- CA
- Canada
- Prior art keywords
- lubricant
- composition
- liquid medium
- aqueous alkaline
- volatile liquid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/32—Esters
- C10M105/38—Esters of polyhydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/32—Esters
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/32—Esters
- C10M105/40—Esters containing free hydroxy or carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/286—Esters of polymerised unsaturated acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/287—Partial esters
- C10M2207/289—Partial esters containing free hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/24—Metal working without essential removal of material, e.g. forming, gorging, drawing, pressing, stamping, rolling or extruding; Punching metal
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/241—Manufacturing joint-less pipes
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/242—Hot working
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/243—Cold working
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/244—Metal working of specific metals
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/244—Metal working of specific metals
- C10N2040/245—Soft metals, e.g. aluminum
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/244—Metal working of specific metals
- C10N2040/246—Iron or steel
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/244—Metal working of specific metals
- C10N2040/247—Stainless steel
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/015—Dispersions of solid lubricants
- C10N2050/02—Dispersions of solid lubricants dissolved or suspended in a carrier which subsequently evaporates to leave a lubricant coating
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
- Shaping Metal By Deep-Drawing, Or The Like (AREA)
Abstract
ABSTRACT
LUBRICATING COMPOSITION AND METHOD
A lubricating composition for press forming consists of a lubricant dissolved or dispersed in a volatile liquid medium, wherein the lubricant comprises at least one ester of a polyhydric alcohol having two or three hydroxyl groups of which one or two are esterified with a long chain carboxylic acid and has a melting point above ambient temperature but low enough to permit removal from a metal surface by an aqueous alkaline cleaner.
The composition is useful for forming structures of shaped aluminium components on a production line.
LUBRICATING COMPOSITION AND METHOD
A lubricating composition for press forming consists of a lubricant dissolved or dispersed in a volatile liquid medium, wherein the lubricant comprises at least one ester of a polyhydric alcohol having two or three hydroxyl groups of which one or two are esterified with a long chain carboxylic acid and has a melting point above ambient temperature but low enough to permit removal from a metal surface by an aqueous alkaline cleaner.
The composition is useful for forming structures of shaped aluminium components on a production line.
Description
LUBRICATING COMPOSITION AND ME~HOD
This invention relates to lubricatlng compositions, particularly those used for press-forming metal sheets. There is current interest in techniques for producing adhesively bonded structures of shaped aluminium components for use in the automotive industry. Such a technique is described for example in EPA 127343. The lubricants of this invention are suitable for use in such techniques.
The technique of converting a coil of aluminium metal sheet into a structure of shaped components for use in the automotive ir.dustry may typically involve the following steps:-- The metal surface is pre-treated to provide a strongly bonded layer thereon which acts as a base for subsequently applied adhesive.
- A lubricant is applied to the treated metal coil. The coil may then be stored or transported, with the lubricant serving to protect the treated metal surface, and is cut up into pieces ready for press-forming.
- The pieces of metal sheet are press-formed into components of desired shape. This and subsequent operations are all performed on an automobile production line.
- Adhesive is applied to selected areas of the shaped cornponents, without first removing the lubricant.
- The components are assembled into the shape of the desired structure, and may be spot welded to give the structure ~reen strength.
- The adhesive is cured at elevated temperature.
- The metal surfaces of the structure are ~:`
~x~
This invention relates to lubricatlng compositions, particularly those used for press-forming metal sheets. There is current interest in techniques for producing adhesively bonded structures of shaped aluminium components for use in the automotive industry. Such a technique is described for example in EPA 127343. The lubricants of this invention are suitable for use in such techniques.
The technique of converting a coil of aluminium metal sheet into a structure of shaped components for use in the automotive ir.dustry may typically involve the following steps:-- The metal surface is pre-treated to provide a strongly bonded layer thereon which acts as a base for subsequently applied adhesive.
- A lubricant is applied to the treated metal coil. The coil may then be stored or transported, with the lubricant serving to protect the treated metal surface, and is cut up into pieces ready for press-forming.
- The pieces of metal sheet are press-formed into components of desired shape. This and subsequent operations are all performed on an automobile production line.
- Adhesive is applied to selected areas of the shaped cornponents, without first removing the lubricant.
- The components are assembled into the shape of the desired structure, and may be spot welded to give the structure ~reen strength.
- The adhesive is cured at elevated temperature.
- The metal surfaces of the structure are ~:`
~x~
subjected ~o an aqueous alkaline cleaner which removes the l~lbrlcant .
- The s~ructure is painted.
A lubricant for use in such a technique needs to fulfil several requirements:
a) The lubricant must, obviously, have suitable lubricating properties for the press-forming operation.
b) The lubrican-t should be solid at li~ely metal storage temperatures. A film Or lubricant that is liquld or sticky is prone to smear and to pick up dust and dirt.
c) Since it is not practicable in a production line to remove lubricant prior to application of adhesive, the lubricant needs to he compatible with the adhesive.
d) After the adhesivs has been applied and cured, the lubricant must be readily removable by an aqueous alkaline cleaner of the type conventionally used to prepare metal surfaces for painting.
There is a need for a lubricant which will fulfil all these requirements. It is an object of the presen~ invention to fulfil that need. However, the luhricants of this invention are likely to be useful, not only for the technique described above, but also for other forming and shaping operations periormed on a variety of metals.
In one aspect, the invention provides a lubricating composition for press forming consisting of a lubricant dissolved or dispersed in a volatlle liquid medium, whereln ~he lubricant comprises at least one ester of a polyhydric alcohol having two or C ,, , ~ .
; ' ' :' ~83~
- The s~ructure is painted.
A lubricant for use in such a technique needs to fulfil several requirements:
a) The lubricant must, obviously, have suitable lubricating properties for the press-forming operation.
b) The lubrican-t should be solid at li~ely metal storage temperatures. A film Or lubricant that is liquld or sticky is prone to smear and to pick up dust and dirt.
c) Since it is not practicable in a production line to remove lubricant prior to application of adhesive, the lubricant needs to he compatible with the adhesive.
d) After the adhesivs has been applied and cured, the lubricant must be readily removable by an aqueous alkaline cleaner of the type conventionally used to prepare metal surfaces for painting.
There is a need for a lubricant which will fulfil all these requirements. It is an object of the presen~ invention to fulfil that need. However, the luhricants of this invention are likely to be useful, not only for the technique described above, but also for other forming and shaping operations periormed on a variety of metals.
In one aspect, the invention provides a lubricating composition for press forming consisting of a lubricant dissolved or dispersed in a volatlle liquid medium, whereln ~he lubricant comprises at least one ester of a polyhydric alcohol having two or C ,, , ~ .
; ' ' :' ~83~
three hydroxyl groups of which one or two are esterifled with a long chain carboxylic acid, wherein the lubricant includes at least one ester having a free hydroxyl group, said lubricant having a melting point above ambient temperature but low enough to permit removal from a me~al surface by an aqueous alkaline cleaner.
In another aspect, the invention provides a method of forming a metal sheet by the steps of applying to the metal sheet a lubricaking composition consisting of a lubricant dissolved or dispersed in a volatile liquid medium, wherein the luhricant comprises at least one ester of a polyhydric alcohol having two or three hydroxyl yroups of which one or two are esterified with a long chain carboxylic acid and has a melting point above ambient tempera~ure but low enough to permit removal from a metal surface by an aqueous alkaline cleaner, removing the volatile liquid medium, and subjecting the metal sheet to a forming operation.
In yet another aspect, the invention provides a method of forming a structure of shaped aluminium components comprising the steps of:
applying to an aluminum shee~ a lubricating composition ~: consisting of a lubricant dissolved or dispersed in a volatile liquid medium, wherein the lubricant comprises at least one ester of a polyhydric alcohol having two or three hydroxyl groups of which one or two are esterified with a long chain carboxylic acid and has a melting point above ambient temperature but low enough to permit removal from a metal suxface by an aqueous alkaline cleaner and removiny the volatile liquid medium, press-forming :. ~
, ~
~''-'. , ' , 33~
3a 20388-1579 pieces of -the sheet into aluminum components, applylng adhesive to the components, bringing the components together in the shape of the desired structure~ and curing the adhesive.
The lubricant is an ester of a polyhydric alcohol with a long-chain carboxylic acid. Dihydric or trihydric alcohols are suitable, ior example ethylene glycol, propylene glycol, diethylene glycol and glycero:L. The long chain carboxylic acid is preferably a saturated straight-chain monocarboxylic acid having from 12 to 18 carbon atoms in the chain, such as lauric, palmitic or stearic acid. The ester may be a full ester, but partial esters containing one or more residual hydroxyl groups in the molecule may be advantageous as described below. Mixtures oE
esters may be used and may be advantageous. The lubricant may con~ain a minor proportion up to 50% of one or more other lubricating compounds, such as long-chain carboxylic acids, esters ~ thereof with monohydric - ~J
~33 alcohols, lon~-chain alcohols and amide and hydrocarbon waxes.
Depending on its intended use, the lubricant may need to be compatible with subsequently applied adhesive. In general, the esters described herein are compatible as a result of being either absorbed or displaced by subsequently applied adhesive without grossly impairing the adhesive bond strength obtainable. By contrast, resinous lubricants and metal soap lubricants are generally not adhesive compatible in this sense. Furthermore, many conventional lubricants are used in the form of aqueous emulsions which contain surface active agents. These can cause problems on storage of lubricated sheet, or in respect of long term adhesion performance, and are preferably absent from compositions according to this invention.
The lubricant has a melting point above ambient temperature, preferably of at least 30 C. This ensures that the lubricant is present as a solid film on the metal substrate, which avoids problems with smearing and blocking during coiling, decoiling, slitting and cutting. The use of such a lubricant avoids contamination of the metal surface with a possibly adhesive-incompatible oil or contaminant and prevents local build up of lubricant to an undesirably thick layer.
The lubricant melts at a-temperature low enough to permit its removal from a metal surface by an aqueous alkaline cleaner, such as is used in automotive production lines to prepare metal parts for painting. The highest practicable temperature for aqueous alkaline cleaners in such circumstances is , , .
~Lif~339~
about 70C. Lubricants melting below 70C and preferably below 65 C. can thus always be removed by aqueous alkaline cleaners. Lubricants melting above 70C may or may not be removable depending on whether they have chemical groups. e.g. hydroxyl groups, which can react with the alkali to assist removal from the metal surface. Thus for example. a commercially available wax having a melting point of 85C and an acid number of 135 to 155 by DIN 53402, was found not to be removable by aqueous alkaline cleaners. On the other hand. glycerol mono-stearate. having a melting point of 81C and two .ree hydroxyl groups per molecule. is removable by aqueous alkaline cleaners.
and falls accordingly within the scope of this invention. A lubricant is deemed removable by aqueous alkaline cleaners if it can be removed by treatment for 2 minutes at 70C with a 15% by weight aqueous solution of Ridoline 16~ (a silicate-based proprietary cleaner marketed by I.C.I. plc) It has been found in general that harder lubricants. give more effective performance in press-forming operations involving stretching. On the other hand. softer lubricants may have superior properties for forming operations involving drawing.
In general. the presence of free hydroxyl groups in the ; molecule increases the hardness of a lubricant.
; Thus. ethylene glycol stearate. diethylene glycol stearate and glycerol stearate are all harder than cyclohexyl stearate. stearyl stearate and similar unhydroxylated esters. The presence of free hydroxyl groups in the lubricant ester thus achieves a double advantage; the lubricant performance. particularly in operations involving stretching. is improved; and ~' ' ~83~
removal from metal surfaces by aqueous alkaline cleaners is made easier. Preferred lubricants for use in this invention are thus hydroxylated esters of polyhydric alcohols with long chain carboxylic acids, and blends of such hydroxylated esters with full esters, the lubricants having melting points in the range 35C to 65 C. There follows a non-exhaustive list of esters suitable for use as lubricants according to this invention. Almost all 1~ these compounds are commercially available for soaps, cosmetics and other non-lubricant uses.
Melting Point Glycerol mono-palmitate 51 -52C
Glycerol di-palmitate 49-57C
15 Glycerol mono-laurate 44C
Ethylene glycol mono-stearate 56-60, 59-65, 65-66C ( 3 grades) Ethylene glycol di-stearate 5~-62, 6~-70C
(2 grades) 20 Propylene glycol mono-stearate 37-42, 33-34C
(2 grades) Propylene glycol di-stearate approx. 52C
Diethylene glycol mono-stearate 43-44C
Diethylene glycol di-stearate 47-52C
25 Glycerol mono-stearate 81C - 74C
The lubricant may be supplied in dispersion in an aqueous medium. More usually, it will be supplied in solution in a hydrocarbon such as xylene. After application of the liquid composition to the metal surface, the volatile liquid is removed by e~aporation leaving a uniform thin film of the solid lubricant.
The volatile liquid concentration is chosen to provide a convenient application viscosity. The rate of ., .
., .' ' ' ' ' ' "~' " '' ': ' 3~
application to the metal surface will depend on the intended use! but may typically be in the range of 1 to 10 g/m2 for aluminium coil to be formed into adhesively bonded structures.
Example-1 Tests were performed to compare two of the lubricants with which this in~ention is concerned with four prior art lubricants, as follows:-Prior art lubricant A is a mineral oil.
Prior art lubricant B is cyclohexyl stearate.
Prior art lubricant C is a commercially available material containing chiefly lauryl laurate with a minor proportion of glycerol monostearate, and is a semi-solid at ambient temperature.
Invention lubricant 1 is based on diethylene glycol monostearate.
Invention lubricant 2 is based on diethylene glycol distearate.
Both the invention lubricants are used in solution in xylene at a convenient application viscosity.
Prior art lubricant D contains ethylene bis-stearamide and lauric acid, and has a melting point of 135C.
To perform the tests, sheets of 5251 alloy (Aluminum Association Inc. Register) of dimensions 26cm x 30cm x 0.~75mm were coated with the described press lubriaants at various coat weights and pressed in a steel die to form a complex shape by a combination of bending, drawing and particularly stretching.
Successful pressing resulted in a drawing-in of the sides of the blank, and the extent of drawing-in indicated the performance of the lubricant. Note was :
~ 8 also taken of whether or not the pressing was split.
Tests were perf'ormed in duplicate, and the results are set in out in the following table:-Lubricant Coatweight Draw-in(mm) Pressing Split(s) g/m2 or not split (ns) 10 Prior Art A 1.7 10.5 s 1.7 11.0 s 3.3 11.5 s 3.3 11.5 s 5.0 10.0 s 5.0 11.0 s Prior Art B 1.7 14.0 s 1.7 15.0 s 3.0 13.0 s 3.0 13.0 s 5.0 14.0 s 5.0 11.0 . s Prior Art C 1.7 15.5 s 1.7 15.5 s :~ 2.7 15.0 s 2.7 15.0 s 5.1 15.5 s 5.1 15.5 s , :
,. ~
~ ~ .
' ' ' ' '' ' 3~
g Lubricant Coatweight Draw-in(mm) Pressing split(s) g/m or not split(ns) Invention 1 1.7 21.0 ns 3.~ ~1.5 ns 3.0 22.0 ns 5.0 21.0 ' ns 5.0 20.0 ns 10 Invention 2 1.7 20.5 ns 1.7 21.0 ns 3.3 21.0 ns 3.3 2~.0 ns 5.0 21.0 ns 5.0 22.0 ns Prior Art D 2.5 22.0 ns 2.5 21.0 ns 5.0 21.0 ns 5.0 21.0 ns The performance of prior art lubricants A, B and C was inferior. The extent of drawing-in of the sides of the blank was rather small and the pressings were all split. By comparison, the performance of prior art lubricant D and of the two invention lubricants was superior. The sides of the blanks were in all cases drawn in to a substantial extent, and the pressings were not split~ In addition, the invention lubricants 1 and 2 were easily removed ~rom the pressings by an aqueous alkaline cleaner of the type normally used in automotive production lines 3~
_ 10 prior to painting. By contrast. prior art lubricant D could not be removed by aqueous alkaline cleaner.
Example 2 Adhesive compatibility was demonstrated by means of salt spray tests. Panels of 5251 alloy were given a 150mg/m chromate-based no-rinse pretreatment.
Lubricant 1 (Example 1) was applied evenly at a lubricant rate of 2.8g/m2 to both surfaces. The panels were cut to give 100mm x 20mm strips. A
proprietary adhesive (Evode Ltd) was applied manually to one lubricated surface. Simple lap shear joints were formed with a 10 x 20mm overlap and drilled by a standard procedure and were left in a salt-spray cabinet. Joint strengths were tested at intervals and 5 were determined to be as follows:-0 weeks 19.0 MPa 4 weeks 17.8 MPa 8 weeks 17.9 MPa These joint strengths are entirely satisfactory, and indicate that the lubricant is adhesive compatible.
3o
In another aspect, the invention provides a method of forming a metal sheet by the steps of applying to the metal sheet a lubricaking composition consisting of a lubricant dissolved or dispersed in a volatile liquid medium, wherein the luhricant comprises at least one ester of a polyhydric alcohol having two or three hydroxyl yroups of which one or two are esterified with a long chain carboxylic acid and has a melting point above ambient tempera~ure but low enough to permit removal from a metal surface by an aqueous alkaline cleaner, removing the volatile liquid medium, and subjecting the metal sheet to a forming operation.
In yet another aspect, the invention provides a method of forming a structure of shaped aluminium components comprising the steps of:
applying to an aluminum shee~ a lubricating composition ~: consisting of a lubricant dissolved or dispersed in a volatile liquid medium, wherein the lubricant comprises at least one ester of a polyhydric alcohol having two or three hydroxyl groups of which one or two are esterified with a long chain carboxylic acid and has a melting point above ambient temperature but low enough to permit removal from a metal suxface by an aqueous alkaline cleaner and removiny the volatile liquid medium, press-forming :. ~
, ~
~''-'. , ' , 33~
3a 20388-1579 pieces of -the sheet into aluminum components, applylng adhesive to the components, bringing the components together in the shape of the desired structure~ and curing the adhesive.
The lubricant is an ester of a polyhydric alcohol with a long-chain carboxylic acid. Dihydric or trihydric alcohols are suitable, ior example ethylene glycol, propylene glycol, diethylene glycol and glycero:L. The long chain carboxylic acid is preferably a saturated straight-chain monocarboxylic acid having from 12 to 18 carbon atoms in the chain, such as lauric, palmitic or stearic acid. The ester may be a full ester, but partial esters containing one or more residual hydroxyl groups in the molecule may be advantageous as described below. Mixtures oE
esters may be used and may be advantageous. The lubricant may con~ain a minor proportion up to 50% of one or more other lubricating compounds, such as long-chain carboxylic acids, esters ~ thereof with monohydric - ~J
~33 alcohols, lon~-chain alcohols and amide and hydrocarbon waxes.
Depending on its intended use, the lubricant may need to be compatible with subsequently applied adhesive. In general, the esters described herein are compatible as a result of being either absorbed or displaced by subsequently applied adhesive without grossly impairing the adhesive bond strength obtainable. By contrast, resinous lubricants and metal soap lubricants are generally not adhesive compatible in this sense. Furthermore, many conventional lubricants are used in the form of aqueous emulsions which contain surface active agents. These can cause problems on storage of lubricated sheet, or in respect of long term adhesion performance, and are preferably absent from compositions according to this invention.
The lubricant has a melting point above ambient temperature, preferably of at least 30 C. This ensures that the lubricant is present as a solid film on the metal substrate, which avoids problems with smearing and blocking during coiling, decoiling, slitting and cutting. The use of such a lubricant avoids contamination of the metal surface with a possibly adhesive-incompatible oil or contaminant and prevents local build up of lubricant to an undesirably thick layer.
The lubricant melts at a-temperature low enough to permit its removal from a metal surface by an aqueous alkaline cleaner, such as is used in automotive production lines to prepare metal parts for painting. The highest practicable temperature for aqueous alkaline cleaners in such circumstances is , , .
~Lif~339~
about 70C. Lubricants melting below 70C and preferably below 65 C. can thus always be removed by aqueous alkaline cleaners. Lubricants melting above 70C may or may not be removable depending on whether they have chemical groups. e.g. hydroxyl groups, which can react with the alkali to assist removal from the metal surface. Thus for example. a commercially available wax having a melting point of 85C and an acid number of 135 to 155 by DIN 53402, was found not to be removable by aqueous alkaline cleaners. On the other hand. glycerol mono-stearate. having a melting point of 81C and two .ree hydroxyl groups per molecule. is removable by aqueous alkaline cleaners.
and falls accordingly within the scope of this invention. A lubricant is deemed removable by aqueous alkaline cleaners if it can be removed by treatment for 2 minutes at 70C with a 15% by weight aqueous solution of Ridoline 16~ (a silicate-based proprietary cleaner marketed by I.C.I. plc) It has been found in general that harder lubricants. give more effective performance in press-forming operations involving stretching. On the other hand. softer lubricants may have superior properties for forming operations involving drawing.
In general. the presence of free hydroxyl groups in the ; molecule increases the hardness of a lubricant.
; Thus. ethylene glycol stearate. diethylene glycol stearate and glycerol stearate are all harder than cyclohexyl stearate. stearyl stearate and similar unhydroxylated esters. The presence of free hydroxyl groups in the lubricant ester thus achieves a double advantage; the lubricant performance. particularly in operations involving stretching. is improved; and ~' ' ~83~
removal from metal surfaces by aqueous alkaline cleaners is made easier. Preferred lubricants for use in this invention are thus hydroxylated esters of polyhydric alcohols with long chain carboxylic acids, and blends of such hydroxylated esters with full esters, the lubricants having melting points in the range 35C to 65 C. There follows a non-exhaustive list of esters suitable for use as lubricants according to this invention. Almost all 1~ these compounds are commercially available for soaps, cosmetics and other non-lubricant uses.
Melting Point Glycerol mono-palmitate 51 -52C
Glycerol di-palmitate 49-57C
15 Glycerol mono-laurate 44C
Ethylene glycol mono-stearate 56-60, 59-65, 65-66C ( 3 grades) Ethylene glycol di-stearate 5~-62, 6~-70C
(2 grades) 20 Propylene glycol mono-stearate 37-42, 33-34C
(2 grades) Propylene glycol di-stearate approx. 52C
Diethylene glycol mono-stearate 43-44C
Diethylene glycol di-stearate 47-52C
25 Glycerol mono-stearate 81C - 74C
The lubricant may be supplied in dispersion in an aqueous medium. More usually, it will be supplied in solution in a hydrocarbon such as xylene. After application of the liquid composition to the metal surface, the volatile liquid is removed by e~aporation leaving a uniform thin film of the solid lubricant.
The volatile liquid concentration is chosen to provide a convenient application viscosity. The rate of ., .
., .' ' ' ' ' ' "~' " '' ': ' 3~
application to the metal surface will depend on the intended use! but may typically be in the range of 1 to 10 g/m2 for aluminium coil to be formed into adhesively bonded structures.
Example-1 Tests were performed to compare two of the lubricants with which this in~ention is concerned with four prior art lubricants, as follows:-Prior art lubricant A is a mineral oil.
Prior art lubricant B is cyclohexyl stearate.
Prior art lubricant C is a commercially available material containing chiefly lauryl laurate with a minor proportion of glycerol monostearate, and is a semi-solid at ambient temperature.
Invention lubricant 1 is based on diethylene glycol monostearate.
Invention lubricant 2 is based on diethylene glycol distearate.
Both the invention lubricants are used in solution in xylene at a convenient application viscosity.
Prior art lubricant D contains ethylene bis-stearamide and lauric acid, and has a melting point of 135C.
To perform the tests, sheets of 5251 alloy (Aluminum Association Inc. Register) of dimensions 26cm x 30cm x 0.~75mm were coated with the described press lubriaants at various coat weights and pressed in a steel die to form a complex shape by a combination of bending, drawing and particularly stretching.
Successful pressing resulted in a drawing-in of the sides of the blank, and the extent of drawing-in indicated the performance of the lubricant. Note was :
~ 8 also taken of whether or not the pressing was split.
Tests were perf'ormed in duplicate, and the results are set in out in the following table:-Lubricant Coatweight Draw-in(mm) Pressing Split(s) g/m2 or not split (ns) 10 Prior Art A 1.7 10.5 s 1.7 11.0 s 3.3 11.5 s 3.3 11.5 s 5.0 10.0 s 5.0 11.0 s Prior Art B 1.7 14.0 s 1.7 15.0 s 3.0 13.0 s 3.0 13.0 s 5.0 14.0 s 5.0 11.0 . s Prior Art C 1.7 15.5 s 1.7 15.5 s :~ 2.7 15.0 s 2.7 15.0 s 5.1 15.5 s 5.1 15.5 s , :
,. ~
~ ~ .
' ' ' ' '' ' 3~
g Lubricant Coatweight Draw-in(mm) Pressing split(s) g/m or not split(ns) Invention 1 1.7 21.0 ns 3.~ ~1.5 ns 3.0 22.0 ns 5.0 21.0 ' ns 5.0 20.0 ns 10 Invention 2 1.7 20.5 ns 1.7 21.0 ns 3.3 21.0 ns 3.3 2~.0 ns 5.0 21.0 ns 5.0 22.0 ns Prior Art D 2.5 22.0 ns 2.5 21.0 ns 5.0 21.0 ns 5.0 21.0 ns The performance of prior art lubricants A, B and C was inferior. The extent of drawing-in of the sides of the blank was rather small and the pressings were all split. By comparison, the performance of prior art lubricant D and of the two invention lubricants was superior. The sides of the blanks were in all cases drawn in to a substantial extent, and the pressings were not split~ In addition, the invention lubricants 1 and 2 were easily removed ~rom the pressings by an aqueous alkaline cleaner of the type normally used in automotive production lines 3~
_ 10 prior to painting. By contrast. prior art lubricant D could not be removed by aqueous alkaline cleaner.
Example 2 Adhesive compatibility was demonstrated by means of salt spray tests. Panels of 5251 alloy were given a 150mg/m chromate-based no-rinse pretreatment.
Lubricant 1 (Example 1) was applied evenly at a lubricant rate of 2.8g/m2 to both surfaces. The panels were cut to give 100mm x 20mm strips. A
proprietary adhesive (Evode Ltd) was applied manually to one lubricated surface. Simple lap shear joints were formed with a 10 x 20mm overlap and drilled by a standard procedure and were left in a salt-spray cabinet. Joint strengths were tested at intervals and 5 were determined to be as follows:-0 weeks 19.0 MPa 4 weeks 17.8 MPa 8 weeks 17.9 MPa These joint strengths are entirely satisfactory, and indicate that the lubricant is adhesive compatible.
3o
Claims (9)
1. A lubricating composition for press forming consisting of a lubricant dissolved or dispersed in a volatile liquid medium, wherein the lubricant comprises at least one ester of a polyhydric alcohol having two or three hydroxyl groups of which one or two are esterified with a long chain carboxylic acid, wherein the lubricant includes at least one ester having a free hydroxyl group said lubricant having a melting point above ambient temperature but low enough to permit removal from a metal surface by an aqueous alkaline cleaner.
2. A composition as claimed in claim 1, wherein the polyhydric alcohol is selected from glycerol, ethylene glycol, propylene glycol and diethylene glycol.
3. A composition as claimed in claim 1 wherein the carboxylic acid is a saturated straight-chain monocarboxylic acid having from 12 to 18 carbon atoms in the chain.
4. A composition as claimed in claim 1, wherein the lubricant has a melting point of from 35°C to 65°C.
5. A composition as claimed in claim 1, wherein the lubricant is present in solution in a volatile hydrocarbon solvent.
6. A composition as claimed in claim 1, wherein the lubricant is compatible with adhesive.
7. A method of forming a metal sheet by the steps of applying to the metal sheet a lubricating composition consisting of a lubricant dissolved or dispersed in a volatile liquid medium, wherein the lubricant comprises at least one ester of a polyhydric alcohol having two or three hydroxyl groups of which one or two are esterified with a long chain carboxylic acid and has a melting point above ambient temperature but low enough to permit removal from a metal surface by an aqueous alkaline cleaner, removing the volatile liquid medium, and subjecting the metal sheet to a forming operation.
8. A method of forming a structure of shaped aluminium components comprising the steps of:
applying to an aluminum sheet a lubricating composition consisting of a lubricant dissolved ox dispersed in a volatile liquid medium, wherein the lubricant comprises at least one ester of a polyhydric alcohol having two or three hydroxyl groups of which one or two are esterified with a long chain carboxylic acid and has a melting point above ambient temperature but low enough to permit removal from a metal surface by an aqueous alkaline cleaner and removing the volatile liquid medium, press-forming pieces of the sheet into aluminum components, applying adhesive to the components, bringing the components together in the shape of the desired structure, and curing the adhesive.
applying to an aluminum sheet a lubricating composition consisting of a lubricant dissolved ox dispersed in a volatile liquid medium, wherein the lubricant comprises at least one ester of a polyhydric alcohol having two or three hydroxyl groups of which one or two are esterified with a long chain carboxylic acid and has a melting point above ambient temperature but low enough to permit removal from a metal surface by an aqueous alkaline cleaner and removing the volatile liquid medium, press-forming pieces of the sheet into aluminum components, applying adhesive to the components, bringing the components together in the shape of the desired structure, and curing the adhesive.
9. A method as claimed in claim 8, comprising the additional step of subjecting the structure to the action of an aqueous alkaline cleaner, and thereafter painting the structure.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB858530146A GB8530146D0 (en) | 1985-12-06 | 1985-12-06 | Lubricating composition |
GB8530146 | 1985-12-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1283901C true CA1283901C (en) | 1991-05-07 |
Family
ID=10589366
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000524630A Expired - Fee Related CA1283901C (en) | 1985-12-06 | 1986-12-05 | Lubricating composition and method |
Country Status (14)
Country | Link |
---|---|
US (1) | US4812248A (en) |
EP (1) | EP0227360B1 (en) |
JP (1) | JPS62181394A (en) |
KR (1) | KR940003501B1 (en) |
CN (1) | CN1009462B (en) |
AU (1) | AU594399B2 (en) |
BR (1) | BR8605980A (en) |
CA (1) | CA1283901C (en) |
DE (1) | DE3679896D1 (en) |
ES (1) | ES2023818B3 (en) |
GB (1) | GB8530146D0 (en) |
IN (1) | IN172014B (en) |
MX (1) | MX168441B (en) |
MY (1) | MY101127A (en) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
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US5248431A (en) * | 1990-02-06 | 1993-09-28 | Dai-Ichi Kogyo Keiyaku Co., Ltd. | Metal working lubricating composition |
US5282990A (en) * | 1990-07-31 | 1994-02-01 | Exxon Chemical Patents Inc. | Synergistic blend of amine/amide and ester/alcohol friction modifying agents for improved fuel economy of an internal combustion engine |
JPH04233998A (en) * | 1990-12-28 | 1992-08-21 | Nippon Parkerizing Co Ltd | Aluminum plate subjected to lubricating treatment and lubrication treating agent for aluminum plate |
US6329329B1 (en) | 1992-10-01 | 2001-12-11 | Alcan International Limited | Lubricated metal workpiece and method |
GB9220719D0 (en) * | 1992-10-01 | 1992-11-11 | Alcan Int Ltd | Lubricated metal workpiece and method |
EP0612832B1 (en) * | 1992-12-07 | 1998-07-22 | Idemitsu Kosan Company Limited | Flame retardant hydraulic oil |
CN1044003C (en) * | 1994-04-12 | 1999-07-07 | 艾尔坎国际有限公司 | Lubricated metal workpiece and method |
US5698502A (en) * | 1996-09-11 | 1997-12-16 | Exxon Chemical Patents Inc | Polyol ester compositions with unconverted hydroxyl groups for use as lubricant base stocks |
WO2001030945A1 (en) * | 1999-10-25 | 2001-05-03 | Nippon Mitsubishi Oil Corporation | Fluid composition for cutting or grinding system employing trace amount of fluid |
US6884762B2 (en) * | 2002-10-28 | 2005-04-26 | Newpark Drilling Fluids, L.L.C. | Ester-containing downhole drilling lubricating composition and processes therefor and therewith |
US7105466B2 (en) * | 2003-08-09 | 2006-09-12 | H.C. Spinks Clay Company, Inc. | Siliceous clay slurry |
US7091148B2 (en) * | 2003-08-09 | 2006-08-15 | H.C. Spinks Clay Company, Inc. | Silicious clay slurry |
US7569525B2 (en) * | 2004-06-23 | 2009-08-04 | Novelis Inc. | Lubricant formulations for sheet metal processing |
JP2008062361A (en) * | 2006-09-11 | 2008-03-21 | Nippon Oil Corp | Ultra-trace oil supply type cutting / grinding method and ultra-trace oil supply type cutting / grinding oil composition |
FR2913356B1 (en) * | 2007-03-08 | 2009-08-14 | Rhodia Recherches & Tech | LUBRICATION WITH DISPERSIONS IN METAL DEFORMATION PROCESSES |
FR2913355B1 (en) * | 2007-03-08 | 2009-08-21 | Michelin Soc Tech | PROCESS FOR WET TREADING WIRE OF STEEL WIRES FOR REINFORCING PNEUMATIC BANDAGES |
US9302312B2 (en) * | 2014-02-07 | 2016-04-05 | GM Global Technology Operations LLC | Lubrication system for warm forming |
CN105127267B (en) * | 2015-10-09 | 2017-05-24 | 黎泽棉 | Drawing forming processing method of tinplate two-piece can, forming die and product thereof |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
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US2126128A (en) * | 1934-05-17 | 1938-08-09 | Harley A Montgomery | Lubricant and method of lubricating metal during forming operations |
US2948681A (en) * | 1955-10-25 | 1960-08-09 | Standard Oil Co | Wire-drawing lubricating composition |
US3468701A (en) * | 1966-02-09 | 1969-09-23 | Atlas Chem Ind | Method of preventing blocking of aluminum sheet material |
US3526596A (en) * | 1968-06-05 | 1970-09-01 | Quaker Chem Corp | Lubricants for metalworking operations |
US4113635A (en) * | 1971-12-13 | 1978-09-12 | Nippon Steel Corporation | Rust-proof lubricant compositions |
US4191658A (en) * | 1974-10-10 | 1980-03-04 | The Lubrizol Corporation | Hot melt metal working lubricants and methods for their application |
WO1979000297A1 (en) * | 1977-11-16 | 1979-05-31 | Nat Can Corp | Method of making metal containers |
US4445813A (en) * | 1977-11-16 | 1984-05-01 | National Can Corporation | Method of forming seamless container |
US4175047A (en) * | 1978-09-25 | 1979-11-20 | Mobil Oil Corporation | Synthetic ester and hydrogenated olefin oligomer lubricant and method of reducing fuel consumption therewith |
ES8204626A1 (en) * | 1980-05-14 | 1982-05-01 | Nat Can Corp | Precoated stock material for containers and method of forming seamless container. |
JPS575777A (en) * | 1980-06-12 | 1982-01-12 | Nissan Motor Co Ltd | Method for bonding part to formed product |
DE3247426A1 (en) * | 1982-12-22 | 1984-06-28 | Merck Patent Gmbh, 6100 Darmstadt | CUTTING OIL FOR THE BARBING PROCESSING OF COLORED METALS |
GB2139538A (en) * | 1983-05-07 | 1984-11-14 | Bl Tech Ltd | Structures fabricated from aluminium components |
GB8502148D0 (en) * | 1985-01-29 | 1985-02-27 | Alcan Int Ltd | Metal-forming lubricant |
-
1985
- 1985-12-06 GB GB858530146A patent/GB8530146D0/en active Pending
-
1986
- 1986-12-02 US US06/937,042 patent/US4812248A/en not_active Expired - Lifetime
- 1986-12-05 AU AU66141/86A patent/AU594399B2/en not_active Ceased
- 1986-12-05 DE DE8686309498T patent/DE3679896D1/en not_active Expired - Fee Related
- 1986-12-05 IN IN1072/DEL/86A patent/IN172014B/en unknown
- 1986-12-05 CA CA000524630A patent/CA1283901C/en not_active Expired - Fee Related
- 1986-12-05 BR BR8605980A patent/BR8605980A/en unknown
- 1986-12-05 ES ES86309498T patent/ES2023818B3/en not_active Expired - Lifetime
- 1986-12-05 EP EP86309498A patent/EP0227360B1/en not_active Expired - Lifetime
- 1986-12-06 KR KR1019860010433A patent/KR940003501B1/en active IP Right Grant
- 1986-12-06 JP JP61291396A patent/JPS62181394A/en active Pending
- 1986-12-06 CN CN86108789A patent/CN1009462B/en not_active Expired
- 1986-12-08 MX MX004583A patent/MX168441B/en unknown
- 1986-12-10 MY MYPI86000192A patent/MY101127A/en unknown
Also Published As
Publication number | Publication date |
---|---|
ES2023818B3 (en) | 1992-02-16 |
EP0227360A1 (en) | 1987-07-01 |
MY101127A (en) | 1991-07-31 |
GB8530146D0 (en) | 1986-01-15 |
CN1009462B (en) | 1990-09-05 |
KR940003501B1 (en) | 1994-04-23 |
JPS62181394A (en) | 1987-08-08 |
EP0227360B1 (en) | 1991-06-19 |
BR8605980A (en) | 1987-09-15 |
MX168441B (en) | 1993-05-25 |
KR870006174A (en) | 1987-07-09 |
US4812248A (en) | 1989-03-14 |
AU6614186A (en) | 1987-06-11 |
CN86108789A (en) | 1987-07-22 |
AU594399B2 (en) | 1990-03-08 |
DE3679896D1 (en) | 1991-07-25 |
IN172014B (en) | 1993-03-13 |
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